about
Treatment of atrial fibrillation by the ablation of localized sources: CONFIRM (Conventional Ablation for Atrial Fibrillation With or Without Focal Impulse and Rotor Modulation) trial.Cell substratum adhesion during early development of Dictyostelium discoideumCollective Signal Processing in Cluster Chemotaxis: Roles of Adaptation, Amplification, and Co-attraction in Collective GuidanceContact inhibition of locomotion determines cell-cell and cell-substrate forces in tissuesInnate non-specific cell substratum adhesionActivated membrane patches guide chemotactic cell motilitySelf-organization in systems of self-propelled particlesModifying Ventricular Fibrillation by Targeted Rotor Substrate Ablation: Proof-of-Concept from Experimental Studies to Clinical VF.Self-organized Vortex State in Two-Dimensional Dictyostelium Dynamics"Self-assisted" amoeboid navigation in complex environmentsModeling Contact Inhibition of Locomotion of Colliding Cells Migrating on Micropatterned SubstratesCO2 Sensing and CO2 Regulation of Stomatal Conductance: Advances and Open QuestionsExcitable waves and direction-sensing in Dictyostelium discoideum: steps towards a chemotaxis modelEmergent Collective Chemotaxis without Single-Cell Gradient SensingClinical mapping approach to diagnose electrical rotors and focal impulse sources for human atrial fibrillationPanoramic electrophysiological mapping but not electrogram morphology identifies stable sources for human atrial fibrillation: stable atrial fibrillation rotors and focal sources relate poorly to fractionated electrograms.Intercellular stress reconstitution from traction force dataComputational mapping identifies localized mechanisms for ablation of atrial fibrillation.Two Independent Mapping Techniques Identify Rotational Activity Patterns at Sites of Local Termination During Persistent Atrial FibrillationA comparison of deterministic and stochastic simulations of neuronal vesicle release models.The role of cell contraction and adhesion in dictyostelium motility.External and internal constraints on eukaryotic chemotaxis.Establishing direction during chemotaxis in eukaryotic cellsDivision accuracy in a stochastic model of Min oscillations in Escherichia coli.Excitation-contraction coupling gain and cooperativity of the cardiac ryanodine receptor: a modeling approach.Polarity mechanisms such as contact inhibition of locomotion regulate persistent rotational motion of mammalian cells on micropatterns.Human atrial fibrillation initiates via organized rather than disorganized mechanisms.Cellular memory in eukaryotic chemotaxis.Gradient sensing in defined chemotactic fieldsDirectional sensing in eukaryotic chemotaxis: a balanced inactivation model.Determining the scale of the Bicoid morphogen gradientRotor stability separates sustained ventricular fibrillation from self-terminating episodes in humansHow input noise limits biochemical sensing in ultrasensitive systems.Noise effects in nonlinear biochemical signaling.Adaptation in a eukaryotic pathway: combining experiments with modelingModeling self-organized spatio-temporal patterns of PIP₃ and PTEN during spontaneous cell polarization.Coupling actin flow, adhesion, and morphology in a computational cell motility model.Structural contributions to fibrillatory rotors in a patient-derived computational model of the atria.Comparison of Detailed and Simplified Models of Human Atrial Myocytes to Recapitulate Patient Specific Properties.Phase synchrony reveals organization in human atrial fibrillation
P50
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P50
name
Wouter-Jan Rappel
@en
type
label
Wouter-Jan Rappel
@en
prefLabel
Wouter-Jan Rappel
@en